Gender diversity in adolescents with polycystic ovary syndrome
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Cintya L. Schweisberger
Abstract
Objectives
The objective of our study was to describe the prevalence of gender diverse (GD) youth among adolescents with polycystic ovary syndrome (PCOS).
Methods
We conducted a retrospective chart review on patients who met NIH criteria for PCOS in our Multidisciplinary Adolescent PCOS Program (MAPP). We compared those with PCOS to MAPP patients who did not meet PCOS criteria as well as to non-PCOS patients from the Adolescent Specialty Clinic (ASC). Variables analyzed included gender identity, androgen levels, hirsutism scores, and mood disorders. We used chi-square, Fisher’s exact, t-tests, and Wilcoxon rank sum tests to compare groups. Gender identities self-reported as male, fluid/both or nonbinary were pooled into the GD category.
Results
Within the MAPP, 7.6% (n=12) of PCOS youth self-identified as GD compared to 1.8% (n=3) of non PCOS youth (p=0.01, chi-square). When compared to non-PCOS GD adolescents from ASC (4.4%; n=3), the difference to PCOS youth was no longer significant (p=0.56). Among MAPP patients, gender diversity was associated with higher hirsutism scores (p<0.01), but not higher androgen levels. In PCOS, depression/anxiety was higher in GD vs cisgender youth (100% vs. 37.6%, p<0.01 and 77.8% vs. 35.8%, p=0.03 respectively).
Conclusions
Gender diversity was observed more commonly in those meeting PCOS criteria. PCOS GD youth were more hirsute and reported more depression/anxiety. Routine screening for differences in gender identity in comprehensive adolescent PCOS programs could benefit these patients, as alternate treatment approaches may be desired to support a transmasculine identity.
Funding source: Canadian Institutes of Health Research
Award Identifier / Grant number: 171268
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Research funding: This study was funded by Canadian Institutes of Health Research (No. 171268).
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: This study was a secondary analysis of data collection with waived consent.
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Ethical approval: The local Institutional Review Board deemed the study exempt from review.
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Articles in the same Issue
- Frontmatter
- Review Article
- Effects of exercise combined with diet intervention on body composition and serum biochemical markers in adolescents with obesity: a systematic review and meta-analysis
- Mini Review
- Effect of stimulants on final adult height
- Original Articles
- Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolism
- The long-term growth, cost-effectiveness, and glycemic effects of growth hormone therapy on children born small for gestational age over 10 years: a retrospective cohort study
- Standard and high dose ergocalciferol regimens for treatment of hypovitaminosis D in epileptic children and adolescents
- Children and adolescents with type 1 diabetes mellitus in Nigeria: clinical characteristics and compliance with care
- Disordered eating and behaviors among young Egyptians with type 1 diabetes: risk factors and comorbidities
- Normal or elevated prolactin is a good indicator to show pituitary stalk interruption syndrome in patients with multiple pituitary hormone deficiency
- No pubertal growth spurt, rapid bone maturation, and menarche post GnRHa treatment in girls with precocious puberty
- Genetic analysis of failed male puberty using whole exome sequencing
- Gender diversity in adolescents with polycystic ovary syndrome
- Case Reports
- Management challenges of Rabson Mendenhall syndrome in a resource limited country: a case report
- Thyroid function tests of iodine deficiency goiter can mimic thyroid hormone resistance alpha
- Pseudohypoaldosteronism associated with hypertrophic cardiomyopathy, hypertension and thrombocytosis due to mutation in the ELAC2 gene: a case report
- Acromicric dysplasia due to a novel missense mutation in the fibrillin 1 gene in a three-generation family
- A case of severe systemic type 1 pseudohypoaldosteronism with 10 years of evolution
- Advantages of monitoring rT3 and dividing LT3 dose in the treatment of consumptive hypothyroidism associated with infantile hepatic hemangioma